Cargando…

Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health

Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here,...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Zhong, Yang, Tianjie, Friman, Ville-Petri, Xu, Yangchun, Shen, Qirong, Jousset, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598729/
https://www.ncbi.nlm.nih.gov/pubmed/26400552
http://dx.doi.org/10.1038/ncomms9413
_version_ 1782394119347240960
author Wei, Zhong
Yang, Tianjie
Friman, Ville-Petri
Xu, Yangchun
Shen, Qirong
Jousset, Alexandre
author_facet Wei, Zhong
Yang, Tianjie
Friman, Ville-Petri
Xu, Yangchun
Shen, Qirong
Jousset, Alexandre
author_sort Wei, Zhong
collection PubMed
description Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here, we experimentally test how the underlying resource competition networks of resident bacterial communities affect invasion resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphere. We find that bipartite resource competition networks are better predictors of invasion resistance compared with resident community diversity. Specifically, communities with a combination of stabilizing configurations (low nestedness and high connectance), and a clear niche overlap with the pathogen, reduce pathogen invasion success, constrain pathogen growth within invaded communities and have lower levels of diseased plants in greenhouse experiments. Bacterial resource competition network characteristics can thus be important in explaining positive diversity–invasion resistance relationships in bacterial rhizosphere communities.
format Online
Article
Text
id pubmed-4598729
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Pub. Group
record_format MEDLINE/PubMed
spelling pubmed-45987292015-10-21 Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health Wei, Zhong Yang, Tianjie Friman, Ville-Petri Xu, Yangchun Shen, Qirong Jousset, Alexandre Nat Commun Article Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here, we experimentally test how the underlying resource competition networks of resident bacterial communities affect invasion resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphere. We find that bipartite resource competition networks are better predictors of invasion resistance compared with resident community diversity. Specifically, communities with a combination of stabilizing configurations (low nestedness and high connectance), and a clear niche overlap with the pathogen, reduce pathogen invasion success, constrain pathogen growth within invaded communities and have lower levels of diseased plants in greenhouse experiments. Bacterial resource competition network characteristics can thus be important in explaining positive diversity–invasion resistance relationships in bacterial rhizosphere communities. Nature Pub. Group 2015-09-24 /pmc/articles/PMC4598729/ /pubmed/26400552 http://dx.doi.org/10.1038/ncomms9413 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wei, Zhong
Yang, Tianjie
Friman, Ville-Petri
Xu, Yangchun
Shen, Qirong
Jousset, Alexandre
Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title_full Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title_fullStr Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title_full_unstemmed Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title_short Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
title_sort trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598729/
https://www.ncbi.nlm.nih.gov/pubmed/26400552
http://dx.doi.org/10.1038/ncomms9413
work_keys_str_mv AT weizhong trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth
AT yangtianjie trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth
AT frimanvillepetri trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth
AT xuyangchun trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth
AT shenqirong trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth
AT joussetalexandre trophicnetworkarchitectureofrootassociatedbacterialcommunitiesdeterminespathogeninvasionandplanthealth